A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201496



Internal ID20768536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149562801..149566500hg38UCSC Ensembl
chr1:148764738..148788781hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg383700
hg1924044
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327602
Supporting Variants
Samples
Known GenesLOC101929780
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201496
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.01216


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